Zobrazeno 1 - 10
of 10
pro vyhledávání: '"J G, Mainz"'
Publikováno v:
Der Pneumologe. 19:104-110
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::8f58cef7fe151784dfe65c4e249cbdf9
https://doi.org/10.1007/s10405-022-00436-2
https://doi.org/10.1007/s10405-022-00436-2
Autor:
Markus A. Rose, J. G. Mainz
Publikováno v:
Monatsschrift Kinderheilkunde. 166:201-211
Die akute nicht-allergieassoziierte Rhinosinusitis (ARS) ist eine haufige Entzundung der Nasen- und Nasenebenhohlenschleimhaute, die typischerweise nach viraler Infektion der oberen Atemwege auftritt und meistens – therapieunabhangig – binnen 10
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::6e94bac74e9a27ccb1f9a48d2a68e58e
https://doi.org/10.1007/s00112-018-0444-z
https://doi.org/10.1007/s00112-018-0444-z
Autor:
C, Schwarz, B, Schulte-Hubbert, J, Bend, M, Abele-Horn, I, Baumann, W, Bremer, F, Brunsmann, D, Dieninghoff, O, Eickmeier, H, Ellemunter, R, Fischer, J, Grosse-Onnebrink, J, Hammermann, H, Hebestreit, M, Hogardt, C, Hügel, M, Hug, S, Illing, A, Jung, B, Kahl, A, Koitschev, R, Mahlberg, J G, Mainz, F, Mattner, A, Mehl, A, Möller, C, Muche-Borowski, T, Nüßlein, M, Puderbach, S, Renner, E, Rietschel, F C, Ringshausen, S, Schmidt, L, Sedlacek, H, Sitter, C, Smaczny, B, Tümmler, R, Vonberg, M O, Wielpütz, H, Wilkens, B, Wollschläger, J, Zerlik, U, Düesberg, S, van Koningsbruggen-Rietschel
Publikováno v:
Pneumologie (Stuttgart, Germany). 72(5)
Cystic Fibrosis (CF) is the most common autosomal-recessive genetic disease affecting approximately 8000 people in Germany. The disease is caused by mutations in the Cystic Fibrosis Transmembrane Conductance Regulator (CFTR) gene leading to dysfuncti
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6f44773f4a4e349d1c30d91dcdb6f1e0
https://pubmed.ncbi.nlm.nih.gov/29758578
https://pubmed.ncbi.nlm.nih.gov/29758578
Autor:
J M, Bock, M, Schien, C, Fischer, L, Naehrlich, M, Kaeding, O, Guntinas-Lichius, A, Gerber, C, Arnold, J G, Mainz
Publikováno v:
Pediatric pulmonology. 52(2)
Cystic fibrosis (CF) patients almost regularly reveal sinonasal pathology. The purpose of this study was to assess association between objective and subjective measurements of sinonasal involvement comparing nasal airflow obtained by active anterior
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::2368a7f3cfecc62f1ba1b81785bd0145
https://pubmed.ncbi.nlm.nih.gov/27893197
https://pubmed.ncbi.nlm.nih.gov/27893197
Publikováno v:
HNO. 63(11)
In cystic fibrosis (CF) mucociliary clearance of the entire respiratory system is impaired. This allows pathogens, such as Pseudomonas aeruginosa to persist and proliferate, which by progressive pulmonary destruction causes 90 % of premature deaths d
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::0a89eb003df85dca4543128e55b9f05e
https://pubmed.ncbi.nlm.nih.gov/26495450
https://pubmed.ncbi.nlm.nih.gov/26495450
Publikováno v:
Zeitschrift fur Geburtshilfe und Neonatologie. 219(4)
Life expectancy and quality of life of cystic fibrosis (CF) patients have been steadily increasing for many decades, due to intensified therapy and research. Correspondingly, the number of pregnancies in women with CF rises. Often it is not possible
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::6fc6d180adab8bb85e13418b1de48b95
https://pubmed.ncbi.nlm.nih.gov/26039502
https://pubmed.ncbi.nlm.nih.gov/26039502
Publikováno v:
HNO. 57(8)
We present the case of a 44-year-old wrestler suffering from persistent bronchitis and chronic rhinosinusitis which had been refractory to therapy. The patient underwent extensive diagnostic examinations throughout the disease. Recently, at the age o
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::46ad76595c0843559e0f0524165fb630
https://pubmed.ncbi.nlm.nih.gov/19609494
https://pubmed.ncbi.nlm.nih.gov/19609494
Publikováno v:
Pneumologie (Stuttgart, Germany). 63(4)
We present the case of a female CF-patient with primary mild disease and pancreatic sufficiency. She did not attend any CF centres for long periods of time. With progression of the disease, she was referred to our thoracic surgery centre for lung tra
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=pmid________::648b22e3cca7b90cacebfc11cffb6c56
https://pubmed.ncbi.nlm.nih.gov/19194840
https://pubmed.ncbi.nlm.nih.gov/19194840
Publikováno v:
Thorax. 65:278-279
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_________::5034dd3658be82fc993a3f4bd0744d0a
https://doi.org/10.1136/thx.2009.125526
https://doi.org/10.1136/thx.2009.125526